Polymer conjugates of mutated neublastin

Drug – bio-affecting and body treating compositions – Solid synthetic organic polymer as designated organic active... – Aftertreated polymer

Reexamination Certificate

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C514S012200, C525S054100, C530S399000

Reexamination Certificate

active

07442370

ABSTRACT:
A dimer comprising a mutated neublastin polypeptide coupled to a polymer is disclosed. Such dimers exhibit prolonged bioavailability and, in preferred embodiments, prolonged biological activity relative to wild-type forms of neublastin.

REFERENCES:
patent: 4883666 (1989-11-01), Sabel et al.
patent: 5084350 (1992-01-01), Chang et al.
patent: 5194596 (1993-03-01), Tischer et al.
patent: 5284761 (1994-02-01), Aebischer et al.
patent: 5350836 (1994-09-01), Kopchick et al.
patent: 5414135 (1995-05-01), Snow et al.
patent: 5496804 (1996-03-01), Reed et al.
patent: 5618531 (1997-04-01), Cherksey
patent: 5733729 (1998-03-01), Lipshutz et al.
patent: 5754524 (1998-05-01), Wark
patent: 5770577 (1998-06-01), Fandl et al.
patent: 5795716 (1998-08-01), Chee et al.
patent: 5800992 (1998-09-01), Fodor et al.
patent: 5834029 (1998-11-01), Bellamkonda et al.
patent: 5846935 (1998-12-01), Panayotatos
patent: 5916555 (1999-06-01), Lee et al.
patent: 5939524 (1999-08-01), Bowditch et al.
patent: 6284540 (2001-09-01), Milbrandt et al.
patent: 6593133 (2003-07-01), Johansen et al.
patent: 6734284 (2004-05-01), Johansen et al.
patent: 2002/0055467 (2002-05-01), Johansen et al.
patent: 2004/0077543 (2004-04-01), Sah et al.
patent: 2004/0142418 (2004-07-01), Sah et al.
patent: 2004/0265972 (2004-12-01), Weintraub et al.
patent: WO 93/06116 (1993-04-01), None
patent: WO 97/08196 (1997-03-01), None
patent: WO 97/11964 (1997-04-01), None
patent: WO 98/32869 (1998-07-01), None
patent: WO 99/03887 (1999-01-01), None
patent: WO 99/43813 (1999-09-01), None
patent: WO 00/01815 (2000-01-01), None
patent: WO 00/04050 (2000-01-01), None
patent: WO 00/18799 (2000-04-01), None
patent: WO 00/34475 (2000-06-01), None
patent: WO 00/73348 (2000-12-01), None
patent: WO 02/051433 (2002-07-01), None
patent: WO 02/060929 (2002-08-01), None
patent: WO 02/072826 (2002-09-01), None
patent: WO 02/078730 (2002-10-01), None
Vukicevic et al., 1996, PNAS USA 93:9021-9026.
Baudet et al., Development 127:4335-4344, 2000.
Choh, PNAS 77(6):3211-14, 1990.
Skolnick et al., 18(1):34-39, 2000.
Watabe et al., J. Neurosci. Res., 41:279-90, 1995.
Matsushita et al., Gene 203, 149-157, 1997.
PIR—80 Accession No. 14968.
Lin et al., Science 260(5111):1130-32, May 21, 1993.
Airaksmen et al. (1999), GDNF family neurotrophic factor signaling: four masters, one servant,Mol Cell Neurosci, 13:313-325.
Atschul et al. (1997), “Gapped BLAST and PSI-BLAST: a new generation of protein database search programs,”Nucl. Acids Res., 25:3389-3402.
Baloh, R.H. et al. (1998), “Artemm, a novel member of the GDNF ligand family, supports peripheral and central neurons and signals through the GFRα3-RET receptor complex,”Neuron, 21:1291-1302.
Baloh, R.H. et al. (2000), “Functional mapping of receptor specificity domains of glial cell line-derived neurotrophic factor (GDNF) family ligands and production of GFRalphail RET-specific agonists,”Journal of biological Chemistry, 275(5):3412-3420.
Borodovsky et al. (1995), “Detection of new genes in a bacterial genome using Markov models for three gene classes,”Nucl. Acids Res., 23:3554-3562.
Daopin et al. (1993), “Chrystal structure of TGF-β2 refined at 1.8 A resolution,”Proteins, 17:176-192.
Delgado, C. et al., (1992), “The uses and properties of PEG-Linked proteins,”Critical Reviews in Therapeutic Drug Carrier Systems, 9(3/4):249-304.
Eigenbrot and Gerber (1997), “X-ray structure of glial cell-derived neurotrophic factor at 1 9 A resolution and implications for receptor binding,”Nat. Struct. Biol., 4:435-438.
Finsen et al. (1992), “Somatostatin and neuropeptide Y in organotypic slice cultures of the rat hippocampus: an immunocytochemical and in situ hybridization study,”Neurosci, 47:105-113.
Francis, G.E., et al., (1998), “Pegylation of Cytokines and other therapeutic proteins and peptides: the importance of biological optimization of coupling techniques,”Int'l. Journal of Hematology, Elsevier Science Publishers, NL., 68(1):1-18.
GenBank™ Accession No. AA844072 (1998).
Lapchak (1977), “Therapeutic potential for glial cell line-derived neurotropic factor (GDNF) based upon pharmacological activities in the CNS,”Rev. Neurosci., 7:165-176).
Lapchak et al. (1996), “Pharmacological characterization of glial cell line-derived neurotrophic factor (GDNF): implications for GDNF as a therapeutic molecule for treating neurodegenerative diseases,”Cell Tissue Res., 286:179-189.
Lin et al. (1993), GDNF: A glial cell line-derived neurotrophic factor for midbrain dopaminergic neurons,Science, 260:1130-1132.
Lorenz et al. (1996), “Heteromultimeric CLC chloride channels with novel properties,”Proc. Natl. Acad. Sci USA, 93: 13362-13366.
Massague et al. (1994), “The TGF-β family and its composite receptor,”Trends Cell Biol., 4:172-178.
Masure et al. (1999), “Enovin, a member of the glial cell-line-derived neurotrophic factor (GDNF) family with growth promoting activity on neuronal cells,”Eur. J. Biochem, 266:892-902.
McDonald and Hendrickson (1993), “A structural superfamily of growth factors containing a cystine knot motif.,”Cell, 73:421-424.
Milbrandt et al. (1998), Persephin, a novel neurotrophic factor related to GDNF and neurturin,Neuron, 20:245-253.
Reddy, K.R. (2000), “Controlled-release peylation, liposomal formulations: new mechanisms in the delivery of injectable drugs,”Annals of Pharmacotherapy, 34(7/8):915-923.
Robertson and Manson (1997), “The GDNF-RET signaling in partnership,”Trends Genet., 13:1-3.
Saarma and Sariola (1999),Microscopy Res.&Technique, 45:292-302.
Sanicola et al. (1997), “Glial cell line-derived neurotrophic factor-dependent RET activation can be mediated by two different cell-surface accessory proteins,”Proc Natl Acad Sci USA, 94:6238-6243.
Sauer and Oertel (1994), “Progressive degeneration of nigrostriatal dopamine neurons following intrastraiatal terminal lesions with 6-hydroxydopamine: a combined retrograde tracing and immunocytochemical study in the rat,”Neuroscience, 59:401-415.
Slooth and Gramsbergen (1995), “Detection of salicylate and its hydroxylated adducts 2.3- and 2.5- dihydroxybenzoic acids as possible indices for in vivo hydroxyl radical formation in combination with catechol- and indoleamines and their metabolites in cerebrospinal fluid and brain tissue,”J. Neurosci. Meth., 60:141-149.
Stoppini et al. (1991), “A simple method for organotypic cultures of nervous tissue,”J. Neurosci. Methods, 37:173-182.
Thompson et al. (1997), “The ClustalX windows interface: flexible strategies for multiple sequence alignment aided by quality analysis tools,”Nucl. Acids Res., 25:4876-4882.
Unsicker (1996), “GDNF: a cytokine at the interface of TGF-betas and neurotrophins,”Cell Tissue Res., 286:175-178.
Von Schwedler et al. (1993), “Vif is crucial for human immunodeficiency virus type 1 proviral DNA synthesis in infected cells,”J. Virol., 67:4945-4955.
Zufferey et al. (1997), “Multiply attenuated lentiviral vector achieves efficient gene delivery in vivo,”Nat. Biotechnol., 15:871-875.
Rosenblad, C., et al., “In Vivo Protection of Nigral Dopamine Neurons by Lentiviral Gene Transfer of the Novel GDNF-Family Member Neublastin/Artemin,”Molecular and Cellular Neuroscience15:199-214 (2000).

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